In humans, two SNPs, rs17819126 in DNAAF4 and rs8053211 in ATP2C2, represented the only correction stable results in an association screen of ten candidate genes tagged by 23 independent SNPs for event-related potential mismatch response, an indicator for auditory discrimination capabilities in dyslexia patients (Müller et al., 2017). Here, ATP2C2 is linked to dyslexia.